Pax Two A

Pax Two A, commonly written Pax2a, is a developmental gene that encodes a paired box transcription factor, a DNA-binding protein that helps establish cell identity during embryogenesis. Pax2a works by binding regulatory DNA sequences and controlling the expression of genes involved in tissue specification, particularly during the formation of sensory structures and the urinary system. In biology, studying Pax2a helps researchers understand gene regulatory networks, embryonic patterning, and organ development. Experimental manipulation of Pax2a expression can reveal how developmental signals guide differentiation and can provide insight into genetic disorders associated with altered PAX2-related function.

Pax Two A - Related Videos

Research

JoVE Journal - Developmental Biology

Identification of Skeletal Muscle Satellite Cells by Immunofluorescence with Pax7 and Laminin Antibodies

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Cited by 23 •

2018

The precise identification of satellite cells is essential for studying their functions under various physiological and pathological conditions. This article presents a protocol to identify satellite cells on adult skeletal muscle sections by immunofluorescence-based staining.

A Microfluidic Device for Quantifying Bacterial Chemotaxis in Stable Concentration Gradients

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Cited by 7 •

2010

This protocol describes the development of a microfluidic device for investigating bacterial chemotaxis in stable concentration gradients of chemoeffectors.

Research

JoVE Journal - Biology
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Manipulation of Rhythmic Food Intake in Mice Using a Custom-Made Feeding System

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2022

Restricting the timing of food intake has emerged as a promising intervention to attenuate diet-induced metabolic diseases. This manuscript details the construction and use of an efficient system built in-house for measuring and manipulating rhythmic food intake in mice.

Research

JoVE Journal - Biology
Free Sample

Isolation of Skeletal Muscle Satellite Cells for In Vitro Myogenesis Studies

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2026

This protocol provides a standardized method for isolating and enriching primary myoblasts from adult and neonatal mouse skeletal muscle through tissue dissociation, sequential filtration, preplating, and defined culture conditions, enabling the establishment and maintenance of satellite cell-derived myoblast cultures for downstream experimental applications.

Synthesis of an Intein-mediated Artificial Protein Hydrogel

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Cited by 2 •

2014

We present the synthesis of a split-intein-mediated protein hydrogel. The building blocks of this hydrogel are two protein copolymers each containing a subunit of a trimeric protein that serves as a crosslinker and one half of a split intein. Mixing of the two protein copolymers triggers an intein trans-splicing reaction, yielding a polypeptide unit that self-assembles into a hydrogel. This hydrogel is highly pH- and temperature-stable, compatible with organic solvents, and easily incorporates...

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